chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	17496248	17496249	T	A	40	GENIC	homozygous	111745378
16	17496911	17496912	A	T	56	GENIC	homozygous	111745380
16	17497282	17497283	C	T	64	GENIC	homozygous	111745382
16	17498104	17498105	A	C	46	GENIC	possibly homozygous	112149905
16	17501372	17501373	C	A	42	GENIC	homozygous	111745384
16	17501430	17501431	A	G	45	GENIC	homozygous	111745386
16	17502300	17502301	G	A	57	GENIC	homozygous	111745388
16	17502335	17502336	A	G	55	GENIC	homozygous	111745390
16	17502758	17502759	T	G	56	GENIC	homozygous	111745392
16	17504940	17504941	A	G	44	GENIC	homozygous	111745394
16	17504943	17504944	A	C	43	GENIC	homozygous	111745396
16	17504945	17504946	A	G	43	GENIC	homozygous	111745398
16	17506625	17506626	G	A	51	GENIC	homozygous	111745400
16	17507363	17507364	T	G	61	GENIC	homozygous	111745402
16	17507616	17507617	T	C	52	GENIC	homozygous	111745404
16	17508318	17508319	C	T	41	GENIC	homozygous	111745406
16	17498402	17498403	G	A	24	GENIC	possibly homozygous	119098542
16	17501885	17501886	G	A	15	GENIC	homozygous	119098543
16	17508641	17508642	A	G	53	GENIC	homozygous	111745408
16	17509393	17509394	T	G	50	GENIC	homozygous	111745410